Cutting Edge: CD28 and c-Rel-Dependent Pathways Initiate Regulatory T Cell Development

被引:92
作者
Vang, Kieng B. [2 ]
Yang, Jianying [2 ]
Pagan, Antonio J. [1 ]
Li, Lin-Xi [2 ]
Wang, Junmei [3 ]
Green, Jonathan M. [4 ]
Beg, Amer A. [3 ]
Farrar, Michael A. [1 ,2 ]
机构
[1] Univ Minnesota, Ctr Immunol, Dept Microbiol, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Ctr Canc, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
[3] H Lee Moffitt Canc Ctr & Res Inst, Dept Immunol, Tampa, FL 33612 USA
[4] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
KAPPA-B; IMMUNOLOGICAL SYNAPSE; HUMORAL IMMUNITY; FILAMIN-A; COSTIMULATION; INTERLEUKIN-2; EXPRESSION; MICE; REQUIREMENT; ACTIVATION;
D O I
10.4049/jimmunol.0903933
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cell (Treg) development proceeds via a two-step process in which naive CD4(+) thymocytes are first converted into CD4(+)CD25(+)CD122(+)GITR(+)Foxp3(-) Treg progenitors, followed by a second step in which IL-2 converts these Treg progenitors into CD4(+)Foxp3(+) Tregs. The costimulatory molecule CD28 is required for efficient Treg development. However, the stage at which CD28 affects Treg development remains undefined. In this article, we demonstrate that Cd28(-/-) mice lack Treg progenitors. Furthermore, the P(187)YAP motif in the cytoplasmic tail of CD28, which links CD28 to Lck activation, is required for this process. In contrast, the (YMNM)-M-170 motif, which links CD28 to PI3K activation, is not required for Treg progenitor development. Finally, the CD28/Lck pathway was shown to activate the NF-kappa B family of transcription factors. We demonstrate that c-Rel, but not NF-kappa B1, promotes the development of Treg progenitors. Thus, a CD28/c-Rel-dependent pathway is involved in initiating Treg development. The Journal of Immunology, 2010, 184: 4074-4077.
引用
收藏
页码:4074 / 4077
页数:4
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